510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K822575Substantially Equivalent

Leeco T3% Diagnostic Kit

Leeco Diagnostics, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822575 is the FDA 510(k) clearance record for LEECO T3% DIAGNOSTIC KIT, a class II device, cleared for Leeco Diagnostics, Inc. on under FDA product code KHQ (Radioassay, Triiodothyronine Uptake). FDA records list 49 510(k) clearances for Leeco Diagnostics, Inc., from to . As of , FDA records show no recalls naming K822575.

Clearance record

Decision date
Received
(36 days to decision)
Product code
KHQ Radioassay, Triiodothyronine Uptake
Regulation
21 CFR 862.1715
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Leeco Diagnostics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KHQ

Trailing 12 months

FDA records hold no clearances under product code KHQ in the trailing twelve months.

FDA records show no clearances under product code KHQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KHQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260